Are carbon dots cluster-triggered luminogens? How through-space interaction arrangement influence the optical properties of carbon dots
Source abstract
Abstract
The use of non-conventional luminescent materials without conjugated chromophores, known as cluster-triggered emission materials (CLgens), has attracted considerable attention as an environmentally benign and biocompatible alternative to conventional fluorophores. A major challenge in developing these materials is the limited understanding of the mechanisms that govern the formation and fate of their excitons, in particular the interaction of the clusters with each other and their surroundings. In this regard, this study aims to gain insight into this mechanism by unravelling the optical properties of the cluster through an innovative approach where a non-traditional luminescent polymer is converted into carbonized polymer dots (CPDs), allowing tuning of electronic interactions and cluster stiffening. The formation of this type of CPDs leads to an increase in through-space interactions (TSI) when compared to the polymer precursor, driven by stronger spatial interactions enabled by the reduced distances and constraints inherent in the formation of the CPDs. Even more striking were the small differences in spectral features between the precursors and CPDs. The typical spectroscopic features associated with TSI, such as the different excitation and absorption spectra, dependence of the emission spectra on the excitation wavelength, and blue-shift emission in small clusters, were also observed. These observations can only lead to the conclusion that TSI is the most plausible mechanism for the luminescence of these CPDs. This represents a significant breakthrough in understanding the relationship between CLgens and the derived CPDs. Furthermore, it highlights the importance of considering the properties of the precursor in order to avoid misconceptions about the luminescence of these materials, and to adjust their properties accordingly.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Carbon and Quantum Dots Applications · Luminescence and Fluorescent Materials · Photocathodes and Microchannel Plates
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (52)
Show source-provided references
1. Highlighting photonics: looking into the next decade10.1186/s43593-021-00002-y ↗
2. Kitai · 2008
3. Aggregation behaviour of pyrene-based luminescent materials, from molecular design and optical properties to application10.1039/D3CS00251A ↗
4. Renewable resource of aggregation-induced emission materials: from photophysical mechanisms to biomedical applications10.1016/j.ccr.2024.215701 ↗
5. Nonconventional luminophores: characteristics, advancements and perspectives10.1039/D0CS01087A ↗
6. Clusterization-triggered emission: uncommon luminescence from common materials10.1016/j.mattod.2019.08.010 ↗
7. Polymers showing cluster triggered emission as potential materials in biophotonic applications10.1016/j.jphotochemrev.2024.100653 ↗
8. Through-space interactions in clusteroluminescence10.1021/jacsau.1c00311 ↗
9. Hohenberg-kohn theorem for nonlocal external potentials10.1103/PhysRevB.12.2111 ↗
10. NIR clusteroluminescence of non‐conjugated phenolic resins enabled by through‐space interactions
11. Activating electronic delocalization: through-space lone-pair interactions versus hydrogen bonding10.1021/acsmaterialslett.4c01182 ↗
12. Clusterization-triggered emission (CTE): one for all, all for one10.1039/D1QM00808K ↗
13. Clusteroluminescence of unconjugated polymers: a review10.1007/s11237-023-09768-3 ↗
14. Recent progress in nonconventional luminescent macromolecules and their applications10.1021/acs.macromol.4c00186 ↗
15. Non‐conjugated polymer dots with crosslink‐enhanced emission in the absence of fluorophore units10.1002/anie.201504951 ↗
16. Crosslink‐enhanced emission effect on luminescence in polymers: advances and perspectives10.1002/ange.201916591 ↗
17. Confined-domain crosslink-enhanced emission effect in carbonized polymer dots10.1038/s41377-022-00745-4 ↗
18. The formation mechanism of carbonized polymer dots: crosslinking‐induced nucleation and carbonization10.1002/anie.202410519 ↗
19. Formation mechanism of carbon dots: from chemical structures to fluorescent behaviors10.1016/j.carbon.2022.03.058 ↗
20. Unraveling the synthesis-structure-property relationship in aromatic amino acids-derived carbon dots
21. Synthesis, properties, and applications of amphiphilic carbon dots: a review10.1016/j.carbon.2024.119921 ↗
22. A new nanomaterial-carbonized polymer dots and their applications: a review10.1016/j.carbon.2025.120122 ↗
23. Nonconventional fluorescent hyperbranched polymer dots as skin nanocarriers constructed from an olefinic aliphatic AB2-Type monomer10.1021/acsapm.2c01328 ↗
24. Molecular glue strategy: large-scale conversion of clustering-induced emission luminogen to carbon dots10.1021/acsami.8b22605 ↗
25. Clustering-induced white light emission from carbonized polymer dots10.1002/adpr.202170016 ↗
26. Carbon dots self-assembly enables near-infrared emission10.1007/s11426-024-2224-9 ↗
27. Amide (n, π ∗) transitions enabled clusteroluminescence in solid‐state carbon dots
28. Solvent-regulated multicolor-emissive carbon dots and their application in multicolor light-emitting diodes10.1039/D4TC02518K ↗
29. Aminated and amidated structures introduced by ethylenediamine pretreatment endow lignin with bright fluorescence10.1039/D2GC02120J ↗
30. Crosslinking‐induced white light emission of poly (hydroxyurethane) microspheres for white LEDs10.1002/adom.201902176 ↗
31. Unexpected luminescence of non-conjugated biomass-based polymers: new approach in photothermal imaging10.1039/D2TB02033E ↗
32. K. Dueñas-Parro, O. Gulias, M. Agut, F. de la Cruz-Martínez, A. Lara-Sánchez, J. A. Castro-Osma, J.F. García-Reyes, A. Sánchez-Ruiz, C. Martín, S. Nonell, Roger bresolí-obach, Cluster and kill: the use of clustering-triggered emission materials for singlet oxygen photosensitization in antimicrobial photodynamic therapy, Adv. Opt. Mater. 13 (2025) 2402179.https://doi.org/10.1002/adom.202402179.10.1002/adom.202402179 ↗
33. Green synthesis of carbon dots from spent coffee grounds via ball-milling: application in fluorescent chemosensors10.1016/j.jclepro.2023.136250 ↗
34. The importance of surface states in N-doped carbon quantum dots10.1016/j.carbon.2021.06.088 ↗
35. Photosensitizer-conjugated ultrasmall carbon nanodots as multifunctional fluorescent probes for bioimaging10.1021/acs.jpcc.5b11721 ↗
36. Mirror effect in atomic force microscopy profiles enables tip reconstruction10.1038/s41598-020-75785-0 ↗
37. Time-resolved methods in biophysics. 7. Photon counting vs. analogue time-resolved singlet oxygen phosphorescence detection10.1039/b804333g ↗
38. Advances in shell and core engineering of carbonized polymer dots for enhanced applications10.1021/acs.accounts.4c00516 ↗
39. Photoluminescence quantum yield of carbon dots: emission due to multiple centers versus excitonic emission10.1039/D4NA00033A ↗
40. The carbonyl-lock mechanism underlying non-aromatic fluorescence in biological matter10.1038/s41467-023-42874-3 ↗
41. Exploring the mechanisms behind non-aromatic fluorescence with the density functional tight binding method10.1021/acs.jctc.4c00125 ↗
42. Carbon nanodots: toward a comprehensive understanding of their photoluminescence10.1021/ja510183c ↗
43. Tuning the properties of luminescent nitrogen-doped carbon dots by reaction precursors10.1016/j.carbon.2016.01.029 ↗
44. Luminescent carbon quantum dots and their application in cell imaging10.1039/c3nj00366c ↗
45. Controlling carbon nanodot fluorescence for optical biosensing10.1039/C6AN00783J ↗
46. Reactive extrusion synthesis of biobased isocyanate-free hydrophobically modified ethoxylated urethanes with pendant hydrophobic groups10.1021/acssuschemeng.2c03535 ↗
47. Urea-doped carbon dots as fluorescent switches for the selective detection of iodide ions and their mechanistic study10.1039/D1RA04558J ↗
48. Advances in shell and core engineering of carbonized polymer dots for enhanced applications10.1021/acs.accounts.4c00516 ↗
49. Surface functionality and formation mechanisms of carbon and graphene quantum dots10.1016/j.diamond.2020.108101 ↗
50. Quenching of singlet molecular oxygen (1O2) by azide anion in solvent mixtures¶10.1562/0031-8655(2001)074<0760:QOSMOO>2.0.CO;2 ↗
51. Rate constants for the decay and reactions of the lowest electronically excited singlet state of molecular oxygen in solution. An expanded and revised compilation10.1063/1.555965 ↗
52. 1H-Phenalen-1-one-2-sulfonic Acid—An extremely efficient singlet molecular oxygen sensitizer for aqueous media